510(k) K072244 ยท MUH System, X-Ray, Extraoral Source, Digital
PLANMECA PROONE
| Applicant | Planmeca Oy, Helsinki, FI |
| Decision | Substantially Equivalent, Sep 21, 2007 |
| Received | Aug 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072244
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.